“I’ve always lived by the motto ‘live and let live.’ As President of the Thalassemia and Sickle Cell Society (TSCS), I’ve dedicated myself to improving the lives of children suffering from these devastating blood disorders. This journey began with a personal conviction and has evolved into a nationally recognized mission.
Born in Hyderabad to a family that migrated from Rajasthan nearly a century ago, I’ve built my business career as Chairman of the Navadurga Group of Industries and my philanthropic endeavors in this city. TSCS was founded in 1998 by a small group of patients, doctors, and philanthropists determined to provide top-notch treatment and management. Today, we serve over 3600 children daily, offering free services, including a high-quality blood bank, modern diagnostic laboratory, and advanced research center.
What drives me is the smile on a child’s face when they receive the care they need. We’ve expanded beyond Telangana, forming a national network, and actively educate the public about antenatal testing and advocate for better support.
The Thalassemia situation in Telangana is dire, and introducing a Government Order (GO) for antenatal testing is crucial. With proper legislation and support, we can significantly reduce the incidence of this disorder and ensure proper treatment. My journey with TSCS is driven by a simple belief: together, we can make a difference. We’re committed to continuously improving services, embracing advancements, and striving to make our state and country Thalassemia-free. This is not just my story but the story of every child we help, every family we support, and every step towards a healthier future.”
- Chandrakant Agarwal, President of Thalassemia and Sickle Cell Society